SCOPUS 정보 검색 플랫폼

Organic and Biomolecular Chemistry

Volumn 7, Issue 3, 2009, Pages 432-434

Tandem copper-catalysed aryl and alkenyl amination reactions: The synthesis of N-functionalised indoles

(3) Hodgkinson, Roy C a Schulz, Jurgen b Willis, Michael C a

a UNIVERSITY OF OXFORD (United Kingdom)

b MERCK RESEARCH LABORATORIES (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMIDES; AMINES; ORGANIC COMPOUNDS;

ALKENYL; AMINATION REACTIONS; ARYL HALIDES; BOND FORMATIONS; DIAMINE COMPLEXES; EFFECTIVE COUPLINGS;

COPPER;

EID: 58849108959 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/b817254d Document Type: Article

Times cited : (50)

References (54)

1
- 0003995267
- Hartwig in J. F. E. I. Negishi, Wiley-Interscience, New York, pp. 1051
- Reviews: J. F. Hartwig, in Handbook of Organopalladium Chemistry for Organic Synthesis, ed., E. I. Negishi, Wiley-Interscience, New York, 2002, vol. 1, pp. 1051
- (2002) Handbook of Organopalladium Chemistry for Organic Synthesis, Ed.

2
- 20544450502
- A. de Meijere and Wiley-VCH, Weinheim, pp. 699 Reviews:
- L. Jiang, S. L. Buchwald, in Metal-Catalysed Cross-Coupling Reactions, ed., A. de Meijere, and F. Diederich, Wiley-VCH, Weinheim, 2004, pp. 699
- (2004) Metal-Catalysed Cross-Coupling Reactions, Ed.
- Jiang, L.¹ Buchwald In, S.L.² Diederich, F.³

3
- 47749142816
- F. Monnier M. Taillefer Angew. Chem., Int. Ed. 2008 47 3096
- (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 3096
- Monnier, F.¹ Taillefer, M.²

4
- 9644277114
- I. P. Beletskaya A. V. Cheprakov Coord. Chem. Rev. 2004 248 2337
- (2004) Coord. Chem. Rev. , vol.248 , pp. 2337
- Beletskaya, I.P.¹ Cheprakov, A.V.²

5
- 0345708168
- For reports comparing Pd and Cu systems, see:
- S. V. Ley A. W. Thomas Angew. Chem., Int. Ed. 2003 42 5400
- (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 5400
- Ley, S.V.¹ Thomas, A.W.²

6
- 0038579438
- X. Huang K. W. Anderson D. Zim L. Jiang A. Klapars S. L. Buchwald J. Am. Chem. Soc. 2003 125 6653
- (2003) J. Am. Chem. Soc. , vol.125 , pp. 6653
- Huang, X.¹ Anderson, K.W.² Zim, D.³ Jiang, L.⁴ Klapars, A.⁵ Buchwald, S.L.⁶

7
- 0038701001
- C. Enguehard H. Allouchi A. Gueiffier S. L. Buchwald J. Org. Chem. 2003 68 4367
- (2003) J. Org. Chem. , vol.68 , pp. 4367
- Enguehard, C.¹ Allouchi, H.² Gueiffier, A.³ Buchwald, S.L.⁴

8
- 1442300776
- L. L. Joyce G. Evindar R. A. Batey Chem. Commun. 2004 446
- (2004) Chem. Commun. , pp. 446
- Joyce, L.L.¹ Evindar, G.² Batey, R.A.³

9
- 4644297662
- G. Young Cho P. Rémy J. Jansson C. Moessner C. Bolm Org. Lett. 2004 6 3293
- (2004) Org. Lett. , vol.6 , pp. 3293
- Young Cho, G.¹ Rémy, P.² Jansson, J.³ Moessner, C.⁴ Bolm, C.⁵

10
- 7744222516
- Reviews:
- G. Cuny M. Bois-Choussy J. Zhu J. Am. Chem. Soc. 2004 126 14475
- (2004) J. Am. Chem. Soc. , vol.126 , pp. 14475
- Cuny, G.¹ Bois-Choussy, M.² Zhu, J.³

11
- 9744246801
- R. B. Bedford C. S. J. Cazin D. Holder Coord. Chem. Rev. 2004 248 2283
- (2004) Coord. Chem. Rev. , vol.248 , pp. 2283
- Bedford, R.B.¹ Cazin, C.S.J.² Holder, D.³

12
- 0037112673
- Examples:
- A. F. Littke G. C. Fu Angew. Chem., Int. Ed. 2002 41 4176
- (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 4176
- Littke, A.F.¹ Fu, G.C.²

13
- 0034794463
- A. Klapars J. C. Antilla X. Huang S. L. Buchwald J. Am. Chem. Soc. 2001 123 7727
- (2001) J. Am. Chem. Soc. , vol.123 , pp. 7727
- Klapars, A.¹ Antilla, J.C.² Huang, X.³ Buchwald, S.L.⁴

14
- 33748701642
- M. L. Kantam B. P. C. Rao B. M. Choudary R. S. Reddy Synlett 2006 2195
- (2006) Synlett , pp. 2195
- Kantam, M.L.¹ Rao, B.P.C.² Choudary, B.M.³ Reddy, R.S.⁴

15
- 33745160738
- L. D. S. Yadav B. S. Yadav V. K. Rai Synthesis 2006 1868
- (2006) Synthesis , pp. 1868
- Yadav, L.D.S.¹ Yadav, B.S.² Rai, V.K.³

16
- 27944470110
- C. Barberis T. D. Gordon C. Thomas X. Zhang K. P. Cusack Tetrahedron Lett. 2005 46 8877
- (2005) Tetrahedron Lett. , vol.46 , pp. 8877
- Barberis, C.¹ Gordon, T.D.² Thomas, C.³ Zhang, X.⁴ Cusack, K.P.⁵

17
- 34247232757
- General indole synthesis reviews:
- L. Zhu L. Cheng Y. Zhang R. Xie J. You J. Org. Chem. 2007 72 2737
- (2007) J. Org. Chem. , vol.72 , pp. 2737
- Zhu, L.¹ Cheng, L.² Zhang, Y.³ Xie, R.⁴ You, J.⁵

18
- 33746864043
- G. R. Humphrey J. T. Kuethe Chem. Rev. 2006 106 2875
- (2006) Chem. Rev. , vol.106 , pp. 2875
- Humphrey, G.R.¹ Kuethe, J.T.²

19
- 0034615797
- G. W. Gribble J. Chem. Soc., Perkin Trans. 1 2000 1045
- (2000) J. Chem. Soc., Perkin Trans. 1 , pp. 1045
- Gribble, G.W.¹

20
- 0003979828
- Academic Press, London
- R. J. Sunberg, Indoles, Academic Press, London, 1996
- (1996) Indoles
- Sunberg, R.J.¹

21
- 58849165916
- J. J. Li and G. W. Gribble, Elsevier, Oxford
- nd Edition, ed., J. J. Li, and, G. W. Gribble, Elsevier, Oxford, 2007
- (2007) nd Edition, Ed.

22
- 2942609168
- G. Zeni R. C. Larock Chem. Rev. 2004 104 2285
- (2004) Chem. Rev. , vol.104 , pp. 2285
- Zeni, G.¹ Larock, R.C.²

23
- 33751424969
- G. Zeni R. C. Larock Chem. Rev. 2006 106 4644
- (2006) Chem. Rev. , vol.106 , pp. 4644
- Zeni, G.¹ Larock, R.C.²

24
- 22944454156
- S. Cacchi G. Fabrizi Chem. Rev. 2005 105 2873
- (2005) Chem. Rev. , vol.105 , pp. 2873
- Cacchi, S.¹ Fabrizi, G.²

25
- 2942557280
- Selected recent examples of transition metal based indole syntheses:
- I. Nakamura Y. Yamamoto Chem. Rev. 2004 104 2127
- (2004) Chem. Rev. , vol.104 , pp. 2127
- Nakamura, I.¹ Yamamoto, Y.²

26
- 33749158251
- Y. Jia J. Zhu J. Org. Chem. 2006 71 7826
- (2006) J. Org. Chem. , vol.71 , pp. 7826
- Jia, Y.¹ Zhu, J.²

27
- 34247624623
- B. M. Trost A. McClory Angew. Chem., Int. Ed. 2007 46 2074
- (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 2074
- Trost, B.M.¹ McClory, A.²

28
- 33746901222
- M. McLaughlin M. Palucki I. W. Davies Org. Lett. 2006 8 3307
- (2006) Org. Lett. , vol.8 , pp. 3307
- McLaughlin, M.¹ Palucki, M.² Davies, I.W.³

29
- 33846999352
- Y.-Q. Fang R. Karisch M. Lautens J. Org. Chem. 2007 72 1341
- (2007) J. Org. Chem. , vol.72 , pp. 1341
- Fang, Y.-Q.¹ Karisch, R.² Lautens, M.³

30
- 34547187077
- M. Nagamochi Y.-Q. Fang M. Lautens Org. Lett. 2007 9 2955
- (2007) Org. Lett. , vol.9 , pp. 2955
- Nagamochi, M.¹ Fang, Y.-Q.² Lautens, M.³

31
- 38549087936
- T. Jensen H. Pedersen B. Bang-Andersen R. Madsen M. Jørgensen Angew. Chem., Int. Ed. 2008 47 888
- (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 888
- Jensen, T.¹ Pedersen, H.² Bang-Andersen, B.³ Madsen, R.⁴ Jørgensen, M.⁵

32
- 34248204484
- L. Ackermann A. Althammer Angew. Chem., Int. Ed. 2007 46 1627
- (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 1627
- Ackermann, L.¹ Althammer, A.²

33
- 36148978880
- A. J. Fletcher M. N. Bax M. C. Willis Chem. Commun. 2007 4764
- (2007) Chem. Commun. , pp. 4764
- Fletcher, A.J.¹ Bax, M.N.² Willis, M.C.³

34
- 33744799129
- M. C. Willis G. N. Brace T. J. K. Findlay I. P. Holmes Adv. Syn. Catal. 2006 348 851
- (2006) Adv. Syn. Catal. , vol.348 , pp. 851
- Willis, M.C.¹ Brace, G.N.² Findlay, T.J.K.³ Holmes, I.P.⁴

35
- 12344275854
- Related Cu-catalysed syntheses of pyrroles and heteroarylpyrroles have been reported:
- M. C. Willis G. N. Brace I. P. Holmes Angew. Chem., Int. Ed. 2005 44 403
- (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 403
- Willis, M.C.¹ Brace, G.N.² Holmes, I.P.³

36
- 33846972345
- X. Yuan X. Xu X. Zhou J. Yuan L. Mai Y. Li J. Org. Chem. 2007 72 1510
- (2007) J. Org. Chem. , vol.72 , pp. 1510
- Yuan, X.¹ Xu, X.² Zhou, X.³ Yuan, J.⁴ Mai, L.⁵ Li, Y.⁶

37
- 34548181107
- For recent examples of Cu-catalysis employed in aromatic heterocycle synthesis, see:
- R. Martín C. H. Larsen A. Cuenca S. L. Buchwald Org. Lett. 2007 9 3379
- (2007) Org. Lett. , vol.9 , pp. 3379
- Martín, R.¹ Larsen, C.H.² Cuenca, A.³ Buchwald, S.L.⁴

38
- 43449101554
- R. D. Viirre G. Evindar R. A. Batey J. Org. Chem. 2008 73 3452
- (2008) J. Org. Chem. , vol.73 , pp. 3452
- Viirre, R.D.¹ Evindar, G.² Batey, R.A.³

39
- 38349086723
- R. Martín A. Cuenca S. L. Buchwald Org. Lett. 2007 9 5521
- (2007) Org. Lett. , vol.9 , pp. 5521
- Martín, R.¹ Cuenca, A.² Buchwald, S.L.³

40
- 36348982844
- N. Zheng S. L. Buchwald Org. Lett. 2007 9 4749
- (2007) Org. Lett. , vol.9 , pp. 4749
- Zheng, N.¹ Buchwald, S.L.²

41
- 33644758102
- J. Yuen Y.-Q. Fang M. Lautens Org. Lett. 2006 8 653
- (2006) Org. Lett. , vol.8 , pp. 653
- Yuen, J.¹ Fang, Y.-Q.² Lautens, M.³

42
- 35348846488
- C. P. Jones K. W. Anderson S. L. Buchwald J. Org. Chem. 2007 72 7968
- (2007) J. Org. Chem. , vol.72 , pp. 7968
- Jones, C.P.¹ Anderson, K.W.² Buchwald, S.L.³

43
- 13844272578
- L. Ackermann Org. Lett. 2005 7 439
- (2005) Org. Lett. , vol.7 , pp. 439
- Ackermann, L.¹

44
- 34548830666
- A. C. Tadd M. R. Fielding M. C. Willis Tetrahedron Lett. 2007 48 7578
- (2007) Tetrahedron Lett. , vol.48 , pp. 7578
- Tadd, A.C.¹ Fielding, M.R.² Willis, M.C.³

45
- 23644447718
- C.-y. Chen P. G. Dormer J. Org. Chem. 2005 70 6964
- (2005) J. Org. Chem. , vol.70 , pp. 6964
- Chen, C.-Y.¹ Dormer, P.G.²

46
- 34447334169
- B. Lu B. Wang Y. Zhang D. Ma J. Org. Chem. 2007 72 5337
- (2007) J. Org. Chem. , vol.72 , pp. 5337
- Lu, B.¹ Wang, B.² Zhang, Y.³ Ma, D.⁴

47
- 33846123939
- B. Lu D. Ma Org. Lett 2006 8 6115
- (2006) Org. Lett , vol.8 , pp. 6115
- Lu, B.¹ Ma, D.²

48
- 33645910529
- M. Carril R. SanMartin I. Tellitu E. Domínguez Org. Lett. 2006 8 1467
- (2006) Org. Lett. , vol.8 , pp. 1467
- Carril, M.¹ Sanmartin, R.² Tellitu, I.³ Domínguez, E.⁴

49
- 0037178121
- A. Klapars X. Huang S. L. Buchwald J. Am. Chem. Soc. 2002 124 7421
- (2002) J. Am. Chem. Soc. , vol.124 , pp. 7421
- Klapars, A.¹ Huang, X.² Buchwald, S.L.³

50
- 0038276941
- F. Y. Kwong S. L. Buchwald Org. Lett. 2003 5 793
- (2003) Org. Lett. , vol.5 , pp. 793
- Kwong, F.Y.¹ Buchwald, S.L.²

51
- 33745962425
- A. Shafir S. L. Buchwald J. Am. Chem. Soc. 2006 128 8742
- (2006) J. Am. Chem. Soc. , vol.128 , pp. 8742
- Shafir, A.¹ Buchwald, S.L.²

52
- 20844435969
- H. Zhang Q. Cai D. Ma J. Org. Chem. 2005 70 5164
- (2005) J. Org. Chem. , vol.70 , pp. 5164
- Zhang, H.¹ Cai, Q.² Ma, D.³

53
- 0029979566
- G. D. Allred L. S. Liebeskind J. Am. Chem. Soc. 1996 118 2748
- (1996) J. Am. Chem. Soc. , vol.118 , pp. 2748
- Allred, G.D.¹ Liebeskind, L.S.²

54
- 0001572533
- R. Shen J. A. Porco, Jr. Org. Lett. 2000 2 1333
- (2000) Org. Lett. , vol.2 , pp. 1333
- Shen, R.¹ Porco Jr. J., A.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.